chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	5281743	5281744	T	C	79	GENIC	heterozygous	119262731
17	5281758	5281759	C	T	85	GENIC	heterozygous	119262732
17	5281796	5281798	GT		75	GENIC	heterozygous	129416859
17	5281798	5281799	T	C	77	GENIC	heterozygous	111444587
17	5281816	5281817	G	A	75	GENIC	heterozygous	111444589
17	5281834	5281835	C	A	67	GENIC	possibly homozygous	111444591
17	5282585	5282585		T	38	GENIC	homozygous	132908250
17	5282922	5282923	C	T	68	GENIC	homozygous	111158575
17	5284724	5284725	T	G	39	GENIC	homozygous	111158577
17	5287634	5287634		GCCCCCGCCT	9	GENIC	possibly homozygous	133033231
17	5288291	5288292	A	T	44	GENIC	homozygous	111380603
17	5283553	5283554	T	A	48	GENIC	homozygous	111380595
17	5285680	5285681	G	A	45	GENIC	possibly homozygous	111380597
17	5286241	5286242	A	G	50	GENIC	homozygous	111380599
17	5287839	5287840	C	T	35	GENIC	possibly homozygous	111380601
17	5287598	5287599	G	A	14	GENIC	homozygous	111518691
17	5288769	5288769		AC	36	GENIC	homozygous	132908251
17	5289664	5289665	G	C	55	GENIC	homozygous	111380605
17	5289807	5289808	G	T	60	GENIC	possibly homozygous	111380607
17	5290944	5290945	T	C	67	GENIC	possibly homozygous	111158585
17	5293940	5293941	G	A	53	GENIC	homozygous	111380609